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Cochlear® LiteWear Case (LC1, 2 pcs)

by Cochlear Limited

Ref P1347785

Active European Union

CE MDR

Valid until

21 Jan 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier TÜV SÜD Product Service GmbH

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number9321502CP1000LWCaseGQ Basic UDI-DI 09321502043816UDI-DIDate8 Oct 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • G70 078611 0123 Active Reissued

    Technical documentation EU MDR

    Issued
    26 Nov 2025
    Expires
    21 Jan 2031
    Valid from
    22 Jan 2026

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Cochlear™ LiteWear Case
Model / Reference
P1347785
Primary DI / UDI-DI
09321502043816
Basic UDI-DI
9321502CP1000LWCaseGQ
Unit of Use DI
09321502046633
EMDN Code
J0380 Auditory active-implantable devices - accessories
Device Class
Class III
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
AU-MF-000009890
Authorised representative
Cochlear Deutschland GmbH & Co. KG DE-AR-000006034

Other devices from Cochlear Ltd

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Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No